Canonical Allele Identifier: CA183791

Gene: NEXN

Linked Data

• ClinVar Variation Id: 179137
• ClinVar RCV Id: RCV000155922 ; RCV002390360
• dbSNP Id: rs727504658
• gnomAD v4: 1-77936001-T-G
• MyVariant Identifiers: chr1:g.78401686T>G (hg19) ; chr1:g.77936001T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936001T>G , CM000663.2:g.77936001T>G	GRCh38
NC_000001.10:g.78401686T>G , CM000663.1:g.78401686T>G	GRCh37
NC_000001.9:g.78174274T>G	NCBI36
NG_016625.1:g.52487T>G , LRG_442:g.52487T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1430T>G MANE Select	ENSP00000333938.7:p.Ile477Ser
ENST00000330010.12:c.1238T>G	ENSP00000327363.8:p.Ile413Ser
ENST00000334785.11:c.1430T>G	ENSP00000333938.7:p.Ile477Ser
ENST00000342754.5:c.1129T>G
ENST00000480732.2:n.1004T>G
NM_001172309.1:c.1238T>G	NP_001165780.1:p.Ile413Ser
NM_144573.3:c.1430T>G , LRG_442t1:c.1430T>G	NP_653174.3:p.Ile477Ser
XM_005271322.2:c.1430T>G	XP_005271379.1:p.Ile477Ser
XM_005271323.2:c.1388T>G	XP_005271380.1:p.Ile463Ser
XM_005271324.3:c.1238T>G	XP_005271381.1:p.Ile413Ser
XM_005271325.2:c.1251+2522T>G	XP_005271382.1:n.1251+2522T>G
XM_005271326.2:c.1196T>G	XP_005271383.1:p.Ile399Ser
XM_005271327.2:c.1013T>G	XP_005271384.1:p.Ile338Ser
XM_005271322.4:c.1430T>G	XP_005271379.1:p.Ile477Ser
XM_005271323.4:c.1388T>G	XP_005271380.1:p.Ile463Ser
XM_005271324.5:c.1238T>G	XP_005271381.1:p.Ile413Ser
XM_005271325.4:c.1251+2522T>G	XP_005271382.1:n.1251+2522T>G
XM_005271326.4:c.1196T>G	XP_005271383.1:p.Ile399Ser
XM_005271327.4:c.1013T>G	XP_005271384.1:p.Ile338Ser
NM_001172309.2:c.1238T>G	NP_001165780.1:p.Ile413Ser
NM_144573.4:c.1430T>G MANE Select	NP_653174.3:p.Ile477Ser